Descripción de la oferta
Medicine moves forward here. So will you.At PrimeVigilance, patient safety is not one part of the job. It is why we exist.We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marking surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on.That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from.If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you.Job DescriptionThe Junior PV Officer role is a mid senior role that requires previous experience in Pharmacovigilance case processing. It includes:Providing support to other activities undertaken by the project team on behalf of the client and the companyPerforming activities in the scope of ICSR management unit within agreed extent and timeframe (including, but not limited to):Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations,PrimeVigilanceprocedures and in accordance with client specific requirements and timelinesSAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management Plan review)Personal data protectionProduct Quality Complaint handling and interaction with Quality AssuranceMedical Information interactionMedDRA and WHOcodingDatabase Outputs and Reports (including data for monthly reporting to clients)Workflow & resource managementMentoring and training of new and more junior employees within the departmentSupport of PV processes related to the ICSR management withinPrimeVigilanceand also toclientsMore senior colleague may perform tasks assigned as per SOP to more juniorpositionPerforming activities in the scope of ICSR management unit within agreed extent and timeframeSupporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line managerQualificationsRequirements:- Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance- Organization skills, including attention to details and multitasking- Planning and time management- Technical skills- Advanced literacy (MS Office)Additional InformationWhen you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.- Quality: we hold ourselves to the standard patients deserve.- Integrity and trust: we do the right thing, especially when it is hard.- Drive and passion: we care about the outcome, because someone is waiting on it.- Agility and responsiveness: we move quickly, because patients cannot wait.- Belonging: everyone is welcome, and every voice counts.- Collaborative partnerships: we go further by going together.We look forward to welcoming your application.#J-18808-Ljbffr
